Hemopoietic Stem Cell Transplantation in Thalassemia: A Report From the European Society for Blood and Bone Marrow Transplantation Hemoglobinopathy Registry, 2000-2010 Publisher Pubmed



Baronciani D¹ ; Angelucci E¹ ; Potschger U² ; Gaziev J³ ; Yesilipek A⁴ ; Zecca M⁵ ; Orofino MG⁶ ; Giardini C⁷ ; Alahmari A⁸ ; Marktel S⁹ ; De La Fuente J¹⁰ ; Ghavamzadeh A¹¹ ; Hussein AA¹² ; Targhetta C¹ Show All Authors
Source: Bone Marrow Transplantation Published:2016

Abstract

Allogeneic hemopoietic stem cell transplantation (HSCT) is the only method currently available to cure transfusion-dependent thalassemia major that has been widely used worldwide. To verify transplantation distribution, demography, activity, policies and outcomes inside the European Group for Blood and Marrow Transplantation (EBMT), we performed a retrospective non-interventional study, extracting data from the EBMT hemoglobinopathy prospective registry database. We included 1493 consecutive patients with thalassemia major transplanted between 1 January 2000 and 31 December 2010. In total, 1359 (91%) transplants were performed on patients <18 years old, 1061 were from a human leukocyte Ag-identical sibling donor. After a median observation time of 2 years, the 2-year overall survival (OS) and event-free survival (EFS; that is, thalassemia-free survival) were 88±1% and 81±1%, respectively. Transplantation from a human leukocyte Ag-identical sibling offered the best results, with OS and EFS of 91±1% and 83±1%, respectively. No significant differences in survival were reported between countries. The threshold age for optimal transplant outcomes was around 14 years, with an OS of 90-96% and an EFS of 83-93% when transplants were performed before this age. Allogeneic HSCT for thalassemia is a curative approach that is employed internationally and produces excellent results. © 2016 Macmillan Publishers Limited.